Brain tumours Flashcards

1
Q

What are the primary brain tumours that arise in adults?

A
Glioblastoma multiforme
Oligodendroglioma
Meningioma
Hemangioblastoma
Pituitary adenoma
Schwannoma
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2
Q

What is a gliobastoma multiforme?

A

Grade IV astrocytoma; a common and very malignant brain tumour with survival of about 1 year.

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3
Q

Which is the most common adult primary brain tumour?

A

gliobastoma multiforme

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4
Q

Where is a gliobastoma multiforme found?

A

In cerebral hemispheres and may cross corpus callosum

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5
Q

What does a gliobastoma multiforme stain positive for?

A

+ GFAP (astrocyte origin)

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6
Q

gliobastoma multiforme histology

A

pseudopalisading pleomorphic tumor cells border central area of necrosis, hemmorhage or microvascular proliferation

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7
Q

What is an oligodendroglioma?

A

A rare slow growing tumour usually inthe frontal lobes

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8
Q

oligodendroglioma histology

A

Fried egg appearnce of cells with chicken wire capillary pattern

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9
Q

Which is the second most common primary brain tumour of adults?

A

meningioma

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10
Q

Description of meningioma ?

A

Common and usually benign. Occurs near surface of brain in parasaggital region. Extra-axial and may have a dural attachment.

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11
Q

Where do you most commonly find a meningioma?

A

surface of brain in parasaggital region

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12
Q

presentation of meningioma

A

often asymptomatic but may present with seizures or focal neurological signs

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13
Q

treatment of meningioma

A

resection or radiosurgery

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14
Q

Which cell does a meningioma originate from?

A

arachnoid

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15
Q

Meningioma histology

A

spindle cells concentrically arranged in whorled pattern. Psammoma bodies.

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16
Q

Risk factor for meningioma

A

prior radiation to head

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17
Q

Where do hemangioblastomas usually occur?

A

in the cerebellum

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18
Q

which syndrome are hemangioblastomas associaed with

A

VHL syndrome

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19
Q

what may a hemangioblastomas produce?

A

erythropoeitin –» secondary polycythemia

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20
Q

hemangioblastoma histology

A

blood vessel origin - closely arranged thin walled-capillaries with minimal intervening parynchema

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21
Q

Pituitary adenoma presentation

A

Bitemporal hemianopia and potentially symptoms from hormones if producing them (most commonly prolactin)

22
Q

Pituitary adenoma of lactotrophs presentation

A

overproduction of prolactin ->ammenhoria/galactorea, impotence and decreased libido in men, decreased bone density due to decreased estrogen in women

23
Q

Pituitary adenoma of somatotrophs presentation

A

acromegaly and gigantism

24
Q

Pituitary adenoma of corticotrophs presentation

A

ACTH excess -> cushing disease

25
Q

Pituitary adenoma of thyrotrophs presentation

A

hyperthyroidism

26
Q

treatment of pituitary adenoma

A

Dopamine agonists (bromocriptine, cabergoline), transphenoidal resection

27
Q

Schwannomas are usually found where?

A

cerebellopontinge angle - involving both VII and VIII

28
Q

How does a vestibular schwannomas present (one that effects CNVIII)

A

tinnitus and hearing loss

29
Q

What disease are schwannomas associated wtih?

A

NFII

30
Q

What do schwannomas stain positively for?

A

S100+ (schwan cell origin)

31
Q

Schwannoma histology?

A

biphasic, dense, hypercellular areas with spindle cells alternating with hypocellular and myxoid areas

32
Q

What are the childhood primary brain tumours?

A
Pilocytic astrocytoma
Medulloblastoma
Ependymoma
Craniopharyngioma
Pinealoma
33
Q

What is a pilocytic astrocytoma?

A

low-grade astrocytome, the most common brain tumour in kids. Well-circumscribed with good prognosis. Benign.

34
Q

Most common location for a pilocytic astrocytoma?

A

posterior fossa (cerebellum)

35
Q

histology of pilocytic astrocytoma

A

GFAP + (astrocyte origin), rosenthal fibers - eosinophilic corkscrew fibers .

Cystic and solid

36
Q

what does pilocytic astrocytoma stain + for?

A

GFAP

37
Q

What is medulloblastoma?

A

most common malignant brain tumour of childhood. Commonly involve cerebellum.

38
Q

Presentation of medulloblastoma?

A

Can compress the 4th ventricle -> noncommunicating hydrocephalus
->headaches and papilledema.

39
Q

where may a medulloblastoma metastasize to?

A

spinal cord (drop metastasis)

40
Q

a medulloblastoma is a form of what?

A

primitive neuroectodermal tumour

41
Q

histology of medulloblastoma

A

homer-wright rosettes - small blue cells

42
Q

Where is an ependymoma found?

A

4th ventricle

43
Q

complication of ependymoma?

A

hydrocephalus

44
Q

ependymoma histology

A

perivascular pseudorosettes and rod-shaped blepharoplasts (basal ciliary bodies) found near the nucleus

45
Q

What is a craniopharyngioma?

A

Most common childhood supratentorial tumour

46
Q

What may a craniopharyngioma be confused with?

A

pituitary adenoma (both cause bitemporal hemianopia)

47
Q

What is a craniopharyngioma derived from?

A

remnants of Rathke pouch (ectoderm)

48
Q

histology of craniopharyngioma

A

calcification may be seen

Cholesterol crystals found in motor oil like fluid within tumour

49
Q

what is a pinealoma?

A

tumour of the pineal gland that may cause parinaud syndrome

50
Q

which syndrome may a pinealoma cuase?

A

parinaud (compression of tectum -> gaze palsy)

51
Q

presentation of pinealoma

A

patient cant look up, pseudo argyll robertson pupils, obstructive hydrocephalus and precocious puberty in males (may production hcG)